Mechanical Engineer 1

Smith+Nephew•Andover, MA

1d•Hybrid

About The Position

Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. Are you an early career engineer who is passionate about innovation and improving patient outcomes? As a Mechanical Engineer I, you will have the opportunity to contribute to the development of medical technologies that help restore mobility, enhance quality of life, and make a meaningful difference for patients around the world. Working alongside experienced engineers and cross functional teams, you will build your technical expertise while supporting the full product development lifecycle in a collaborative and growth focused environment.

Requirements

Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or a related engineering discipline
0 to 2 years of engineering experience, including internships, co ops, senior design projects, or research experience
Understanding of mechanical design principles and engineering problem solving techniques
Experience using CAD software through academic, project, internship, or personal experience, with SolidWorks experience preferred
Ability to create and interpret engineering drawings, with exposure to GD&T concepts preferred
Knowledge of manufacturing processes, assembly methods, and design for manufacturing and assembly principles
Strong analytical, communication, organizational, and teamwork skills
Demonstrated curiosity, attention to detail, accountability, and a willingness to learn in a fast paced environment
Interest in healthcare technologies and medical device development

Nice To Haves

SolidWorks experience preferred
Exposure to GD&T concepts preferred
Exposure to testing, data analysis, statistics, or design of experiments through coursework or practical experience is preferred

Responsibilities

Support the design and development of mechanical components, assemblies, and medical device systems
Participate in concept development, prototyping, design evaluations, and product improvement activities
Create and maintain CAD models, engineering drawings, and technical documentation
Assist with verification and validation testing, including test method development, execution, data analysis, and reporting
Support troubleshooting activities, root cause investigations, and engineering change implementation
Contribute to risk management activities, design reviews, and maintenance of Design History Files
Collaborate with Manufacturing, Quality, Regulatory, Marketing, Human Factors, and R&D teams to support product development and launch activities
Learn and apply medical device design controls, quality systems, and regulatory requirements
Participate in project meetings and provide technical updates while continuing professional development through training and mentorship